Coprecipitation Method for Preparing Cobalt Oxide (Co3O4) Catalyst to Efficiently Oxidize Ammonia

dc.contributor.author Al-Okla, Mudar
dc.contributor.author Zeidan, Hani
dc.date.accessioned 2025-12-24T21:38:04Z
dc.date.available 2025-12-24T21:38:04Z
dc.date.issued 2025
dc.description.abstract In this study three samples of cobalt oxide were prepared via coprecipitation at pH 9.5 using cobalt nitrate as a precursor. They were dried at 120 degrees C before calcining at 400, 500, and 600 degrees C. The crystalline phases were determined using X-ray diffraction (XRD), revealing the presence of the Co3O4 phase in all prepared samples in varying proportions. Fourier Transform Infrared Spectroscopy (FTIR) spectra showed distinct bands corresponding to the vibrational motion of the Co-O bond, confirming the formation of cobalt oxide (Co3O4). Scanning electron microscope (SEM) analysis of the Co 500 sample revealed particles in the range of 40-350 nm (average similar to 100 nm) with relatively low agglomeration, while energy-dispersive X-ray spectroscopy (EDX) confirmed a composition consistent with stoichiometric Co3O4 (85.7 wt % Co and 13.6 wt % O). Pyridine-adsorbed FTIR spectra indicated that the sample calcined at 500 degrees C possessed the most balanced ratio of Lewis and Br empty set nsted acid sites, which correlated with its highest catalytic activity. The textural properties of all samples were analyzed using nitrogen adsorption data at 77 K, and the adsorption isotherms were found to be type IV, with hysteresis loops indicating capillary condensation in mesopores. The specific surface area reached a maximum of 4.837 m(2)/g for the sample calcined at 500 degrees C. This sample also exhibited the highest total acidity (0.035 mmol/g) and strong acidic sites (the initial electrode potential value E-i = 73.2 mV), which enhanced catalytic performance. Pore radius calculations further revealed that the samples contained mesopores. The catalytic efficiency of the prepared samples in the ammonia oxidation reaction was evaluated at 450 degrees C. The sample calcined at 500 degrees C demonstrated the highest catalytic activity. The sample calcined at 500 degrees C achieved 100% NH3 conversion at 475 degrees C and maintained full activity over 10 consecutive cycles, demonstrating high stability and reusability. en_US
dc.description.sponsorship Department of Chemistry at Idlib University en_US
dc.description.sponsorship We would like to thank the Department of Chemistry at Idlib University for the use of the facilities. en_US
dc.identifier.doi 10.1134/S0023158424602729
dc.identifier.issn 0023-1584
dc.identifier.issn 1608-3210
dc.identifier.scopus 2-s2.0-105021239854
dc.identifier.uri https://doi.org/10.1134/S0023158424602729
dc.identifier.uri https://hdl.handle.net/123456789/12719
dc.language.iso en en_US
dc.publisher Pleiades Publishing Ltd en_US
dc.relation.ispartof Kinetics and Catalysis en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Ammonia Oxidation en_US
dc.subject Catalytic Activity en_US
dc.subject Cobalt Oxide (Co3O4) en_US
dc.subject Co-Precipitation en_US
dc.subject Lewis and Bronsted Acid Sites en_US
dc.subject Textural Properties en_US
dc.title Coprecipitation Method for Preparing Cobalt Oxide (Co3O4) Catalyst to Efficiently Oxidize Ammonia en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.scopusid 59146057100
gdc.author.scopusid 57170829100
gdc.author.wosid Zeidan, Hani/Ist-6827-2023
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department Konya Technical University en_US
gdc.description.departmenttemp [Al-Okla, Mudar; Zeidan, Hani] Idlib Univ, Fac Sci, Dept Appl Chem, Idlib, Syria; [Zeidan, Hani] Konya Tech Univ, Dept Chem Engn, TR-42250 Konya, Turkiye en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q4
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q4
gdc.identifier.openalex W7104447961
gdc.identifier.wos WOS:001611517000001
gdc.index.type WoS
gdc.index.type Scopus
gdc.openalex.collaboration International
gdc.openalex.fwci 0.0
gdc.openalex.normalizedpercentile 0.65
gdc.opencitations.count 0
gdc.plumx.scopuscites 0
gdc.scopus.citedcount 0
gdc.wos.citedcount 0

Files